Multicore Nanoparticles Research Articles

Tailored Magnetic Multicore Nanoparticles for Use as Blood Pool MPI Tracers

For the preclinical development of magnetic particle imaging (MPI) in general, and the exploration of possible new clinical applications of MPI in particular, tailored MPI tracers with surface properties optimized for the intended use are needed. Here we present the synthesis of magnetic multicore particles (MCPs) modified with polyethylene glycol (PEG) for use as blood pool MPI tracers. To achieve the stealth effect the carboxylic groups of the parent MCP were activated and coupled with pegylated amines (mPEG-amines) with different PEG-chain lengths from 2 to 20 kDa. The resulting MCP-PEG variants with PEG-chain lengths of 10 kDa (MCP-PEG10K after one pegylation step and MCP-PEG10K2 after a second pegylation step) formed stable dispersions and showed strong evidence of a successful reaction of MCP and MCP-PEG10K with mPEG-amine with 10 kDa, while maintaining their magnetic properties. In rats, the mean blood half-lives, surprisingly, were 2 and 62 min, respectively, and therefore, for MCP-PEG10K2, dramatically extended compared to the parent MCP, presumably due to the higher PEG density on the particle surface, which may lead to a lower phagocytosis rate. Because of their significantly extended blood half-life, MCP-PEG10K2 are very promising as blood pool tracers for future in vivo cardiovascular MPI.

Curcuminoids-conjugated multicore magnetic nanoparticles: Design and characterization of a potential theranostic nanoplatform

Theranostic systems have gained much attention due to their widespread biological and technological applications. In this work, we report the synthesis and characterization of a theranostic nanoplatform based on multicore magnetic iron oxide functionalized with curcuminoids (CC) and coated with silica (MNP-CC@SiO2). The physicochemical and colloidal properties of the unloaded-curcuminoids nanoplatform (MNP@SiO2) were evaluated by several techniques, including X-ray diffraction, magnetometry measurements, transmission electron microscopy, and zeta potential and dynamic light scattering. The time and maximum loading of curcuminoids onto multicore MNP (MNP-CC) were investigated by adsorption kinetic and isotherm. After the curcuminoids loading, MNP-CC was coated with amorphous silica to prevent pervasion, degradation of the curcuminoids, and providing colloidal stabilization to the system. The resulting MNP-CC@SiO2 exhibits expressive fluorescence, in addition to interesting magnetic and thermal properties. On the other hand, this device shows a negligible release of curcuminoids in sink conditions. The potential theranostic features of MNP-CC@SiO2 nanoplatform are attributed to the combination of a multicore magnetic structure with a silica coating. We argue that this should provide a versatile and multifunctional nanoplatform. It is expected to present potential biomedical applications, such as image contrast, magnetic hyperthermia treatment, cell separation, and drug delivery.

Au@ZIF-8 Core–Shell Nanoparticles as a SERS Substrate for Volatile Organic Compound Gas Detection

Surface-enhanced Raman spectroscopy (SERS) is a promising ultrasensitive analysis technology due to outstanding molecular fingerprint identification. However, the measured molecules generally need to be adsorbed on a SERS substrate, which makes it difficult to detect weakly adsorbed molecules, for example, the volatile organic compound (VOC) molecules. Herein, we developed a kind of a SERS detection method for weak adsorption molecules with Au@ZIF-8 core-shell nanoparticles (NPs). The well-uniformed single- and multicore-shell NPs can be synthesized controllably, and the shell thickness of the ZIF-8 was able to be precisely controlled (from 3 to 50 nm) to adjust the distance and electromagnetic fields between metal nanoparticles. After analyzing the chemical and physical characterization, Au@ZIF-8 core-shell NPs were employed to detect VOC gas by SERS. In contrast with multicore or thicker-shell nanoparticles, Au@ZIF-8 with a shell thickness of 3 nm could efficiently probe various VOC gas molecules, such as toluene, ethylbenzene, and chlorobenzene. Besides, we were capable of observing the process of toluene gas adsorption and desorption using real-time SERS technology. As observed from the experimental results, this core-shell nanostructure has a promising prospect in diverse gas detection and is expected to be applied to the specific identification of intermediates in catalytic reactions.

Engineering Iron Oxide Nanocatalysts by a Microwave-Assisted Polyol Method for the Magnetically Induced Degradation of Organic Pollutants.

Advanced oxidation processes constitute a promising alternative for the treatment of wastewater containing organic pollutants. Still, the lack of cost-effective processes has hampered the widespread use of these methodologies. Iron oxide magnetic nanoparticles stand as a great alternative since they can be engineered by different reproducible and scalable methods. The present study consists of the synthesis of single-core and multicore magnetic iron oxide nanoparticles by the microwave-assisted polyol method and their use as self-heating catalysts for the degradation of an anionic (acid orange 8) and a cationic dye (methylene blue). Decolorization of these dyes was successfully improved by subjecting the catalyst to an alternating magnetic field (AMF, 16 kA/m, 200 kHz). The sudden temperature increase at the surface of the catalyst led to an intensification of 10% in the decolorization yields using 1 g/L of catalyst, 0.3 M H2O2 and 500 ppm of dye. Full decolorization was achieved at 90 °C, but iron leaching (40 ppm) was detected at this temperature leading to a homogeneous Fenton process. Multicore nanoparticles showed higher degradation rates and 100% efficiencies in four reusability cycles under the AMF. The improvement of this process with AMF is a step forward into more sustainable remediation techniques.

Rational design and in-situ formation of nickel–cobalt nitride multi-core/hollow N-doped carbon shell anode for Li-ion batteries

• Nickel–cobalt nitrides with unique multi-core/shell nanostructure are proposed. • Multi-core/shell nanostructures are successfully formed via in-situ thermal annealing process. • Hierarchical composite anodes deliver superior performance for Li-ion batteries. • Structural and morphological evolution at different electrochemical states is elucidated. The construction of a carbon-encapsulated multi-core nanostructure based on transition metal nitride is a preferred approach to efficiently mitigate volume expansion with improved sustainability and to enhance conductivity with more active sites for Li-ion cell reaction. Herein, we report the in-situ formation of carbon-coated nickel–cobalt nitride multi-core nanoparticles encapsulated by hollow N-doped carbon shell via monodispersed Ni 3 [Co(CN) 6 ] 2 Prussian blue analogue/polydopamine precursors using by simultaneous nitridation and calcination process. The (Ni/Co) 3 N multi-core nanoparticles (Ni:Co = 3:2) were highly dispersed in conductive and hollow N-doped carbon shell, thereby (i) mitigating mechanical stress by volume change during the conversion reaction of nitrides, (ii) stabilizing the electrochemical reaction surface with a thin solid electrolyte interphase, and (iii) maintaining the original structure and hierarchical morphologies even after long cycles. The (Ni/Co) 3 N multi-core@hollow N-doped carbon shell demonstrated better electrochemical performance than the (Ni/Co) 3 N@carbon shell without the outer hollow N-doped carbon shell for the Li-ion battery anode, which has an excellent reversible capacity of ~440 mAh g −1 and a stable cycle life of 130 cycles at 200 mA g −1 . The rational synthetic strategy of the unique hybrid nanoarchitecture via in-situ formation of polymer-coated metal–organic frameworks is key in improving the Li-ion storage capacity and cycle stability.

Properties of single- and multi-core magnetic nanoparticles assessed by magnetic susceptibility measurements

Characterization of structural and magnetic properties of MNP ensembles is crucial in tailoring their performance for biomedical applications. In this work, we evaluate the size distribution of magnetic cores in single- and multi-core nanoparticles in water suspension using transmission electron microscopy (TEM) and static magnetization curve, with the geometrical core size ranges from 8.3 to 40.2 nm. A reasonable core size derived from the magnetization curve is obtained in comparison to the geometrical size from TEM image. The magnetic moment distribution possibly reveals that the reduction of effective magnetic core size is due to the magnetization degradation in cores. The hydrodynamic size and average anisotropy energy ratio obtained from the AC susceptibility response of MNPs from 5 Hz to 100 kHz are also evaluated. The complex distribution of relaxation time is constructed by applying a non-negative least square method to an AC susceptibility model that incorporates the inter- and intra-potential-well contributions. It is found that a log-normal distribution might not be adequate to represent the hydrodynamic size distribution reconstructed from the AC susceptibility responses of the suspended samples. It is demonstrated that the AC susceptibility model used in this study can be used to fairly estimate the average anisotropy energy ratio for MNP ensembles dominated by thermally blocked particles. Moreover, it can be suggested that besides the geometrical core size, the degree of core aggregation also plays an important role in determining the anisotropy energy ratio and effective magnetic moment.

From Single-Core Nanoparticles in Ferrofluids to Multi-Core Magnetic Nanocomposites: Assembly Strategies, Structure, and Magnetic Behavior.

Iron oxide nanoparticles are the basic components of the most promising magnetoresponsive nanoparticle systems for medical (diagnosis and therapy) and bio-related applications. Multi-core iron oxide nanoparticles with a high magnetic moment and well-defined size, shape, and functional coating are designed to fulfill the specific requirements of various biomedical applications, such as contrast agents, heating mediators, drug targeting, or magnetic bioseparation. This review article summarizes recent results in manufacturing multi-core magnetic nanoparticle (MNP) systems emphasizing the synthesis procedures, starting from ferrofluids (with single-core MNPs) as primary materials in various assembly methods to obtain multi-core magnetic particles. The synthesis and functionalization will be followed by the results of advanced physicochemical, structural, and magnetic characterization of multi-core particles, as well as single- and multi-core particle size distribution, morphology, internal structure, agglomerate formation processes, and constant and variable field magnetic properties. The review provides a comprehensive insight into the controlled synthesis and advanced structural and magnetic characterization of multi-core magnetic composites envisaged for nanomedicine and biotechnology.

In vivo magnetic particle imaging: angiography of inferior vena cava and aorta in rats using newly developed multicore particles

Magnetic Particle Imaging (MPI) is a new imaging modality, which maps the distribution of magnetic nanoparticles (MNP) in 3D with high temporal resolution. It thus may be suited for cardiovascular imaging. Its sensitivity and spatial resolution critically depend on the magnetic properties of MNP. Therefore, we used novel multicore nanoparticles (MCP 3) for in-vivo MPI in rats and analyzed dose requirements, sensitivity and detail resolution. 8 rats were examined using a preclinical MPI scanner (Bruker Biospin GmbH, Germany) equipped with a separate receive coil. MCP 3 and Resovist were administered intravenously (i.v.) into the rats’ tail veins at doses of 0.1, 0.05 and 0.025 mmol Fe/kg followed by serial MPI acquisition with a temporal resolution of 46 volumes per second. Based on a qualitative visual scoring system MCP 3–MPI images showed a significantly (P ≤ 0.05) higher image quality than Resovist-MPI images. Morphological features such as vessel lumen diameters (DL) of the inferior vena cava (IVC) and abdominal aorta (AA) could be assessed along a 2-cm segment in mesenteric area only after administration of MCP 3 at dosages of 0.1, 0.05 mmol Fe/kg. The mean DL ± SD estimated was 2.7 ± 0.6 mm for IVC and 2.4 ± 0.7 mm for AA. Evaluation of DL of the IVC and AA was not possible in Resovist-MPI images. Our results show, that MCP 3 provide better image quality at a lower dosage than Resovist. MCP 3-MPI with a clinically acceptable dose of 0.05 mmol Fe/kg increased the visibility of vessel lumens compared to Resovist-based MPI towards possible detection of vascular abnormalities such as stenosis or aneurysms, in vivo.

Investigation of magnetically driven passage of magnetic nanoparticles through eye tissues for magnetic drug targeting

This paper elucidates the feasibility of magnetic drug targeting to the eye by using magnetic nanoparticles (MNPs) to which pharmaceutical drugs can be linked. Numerical simulations revealed that a magnetic field gradient of 20 T m−1 seems to be promising for dragging magnetic multicore nanoparticles of about 50 nm into the eye. Thus, a targeting magnet system made of superconducting magnets with a magnetic field gradient at the eye of about 20 T m−1 was simulated. For the proof-of-concept tissue experiments presented here the required magnetic field gradient of 20 T m−1 was realized by a permanent magnet array. MNPs with an optimized multicore structure were selected for this application by evaluating their stability against agglomeration of MNPs with different coatings in water for injections, physiological sodium chloride solution and biological media such as artificial tear fluid. From these investigations, starch turned out to be the most promising coating material because of its stability in saline fluids due to its steric stabilization mechanism. To evaluate the passage of MNPs through the sclera and cornea of the eye tissues of domestic pigs (Sus scrofa domesticus), a three-dimensionally printed setup consisting of two chambers (reservoir and target chamber) separated by the eye tissue was developed. With the permanent magnet array emulating the magnetic field gradient of the superconducting setup, experiments on magnetically driven transport of the MNPs from the reservoir chamber into the target chamber via the tissue were performed. The resulting concentration of MNPs in the target chamber was determined by means of quantitative magnetic particle spectroscopy. It was found that none of the tested particles passed the cornea, but starch-coated particles could pass the sclera at a rate of about 5 ng mm−2 within 24 h. These results open the door for future magnetic drug targeting to the eye.

Static magnetic response of multicore particles.

We present theoretical calculations of the characteristics of the static magnetic response of multicore magnetic nanoparticles. These particles contain a considerable number (∼10^{2}) of single-domain magnetic nanocrystallites, which are modeled as uniformly magnetized balls with uniaxial magnetocrystalline anisotropy, the energetic barrier of which is comparable with the thermal energy. Thus, we model a multicore magnetic nanoparticle as an ensemble of superparamagnetic nanoparticles, the position and the easy magnetization axis of which are fixed but randomly distributed. Summing up the magnetic moments of the nanocrystallites inside a multicore particle, we thus obtain the magnetic moment of the multicore particle under the assumption that magnetic interactions between the nanocrystallites can be neglected. It is found that the weak-field magnetic response of these multicore particles is independent of anisotropy constant. The model is compared with recent experimental data and good agreement is found.

Libraries of Uniform Magnetic Multicore Nanoparticles with Tunable Dimensions for Biomedical and Photonic Applications.

Multicore iron oxide nanoparticles, also known as colloidal nanocrystal clusters, are magnetic materials with diverse applications in biomedicine and photonics. Here, we examine how both of their characteristic dimensional features, the primary particle and sub-micron colloid diameters, influence their magnetic properties and performance in two different applications. The characterization of these basic size-dependent properties is enabled by a synthetic strategy that provides independent control over both the primary nanocrystal and cluster dimensions. Over a wide range of conditions, electron microscopy and X-ray diffraction reveal that the oriented attachment of smaller nanocrystals results in their crystallographic alignment throughout the entire superstructure. We apply a sulfonated polymer with high charge density to prevent cluster aggregation and conjugate molecular dyes to particle surfaces so as to visualize their collection using handheld magnets. These libraries of colloidal clusters, indexed both by primary nanocrystal dimension (dp) and overall cluster diameter (Dc), form magnetic photonic crystals with relatively weak size-dependent properties. In contrast, their performance as MRI T2 contrast agents is highly sensitive to cluster diameter, not primary particle size, and is optimized for materials of 50 nm diameter (r2 = 364 mM-1 s-1). These results exemplify the relevance of dimensional control in developing applications for these versatile materials.

In vivo clearance of 19F MRI imaging nanocarriers is strongly influenced by nanoparticle ultrastructure

Perfluorocarbons hold great promise both as imaging agents, particularly for 19F MRI, and in therapy, such as oxygen delivery. 19F MRI is unique in its ability to unambiguously track and quantify a tracer while maintaining anatomic context, and without the use of ionizing radiation. This is particularly well-suited for inflammation imaging and quantitative cell tracking. However, perfluorocarbons, which are best suited for imaging – like perfluoro-15-crown-5 ether (PFCE) - tend to have extremely long biological retention. Here, we showed that the use of a multi-core PLGA nanoparticle entrapping PFCE allows for a 15-fold reduction of half-life in vivo compared to what is reported in literature. This unexpected rapid decrease in 19F signal was observed in liver, spleen and within the infarcted region after myocardial infarction and was confirmed by whole body NMR spectroscopy. We demonstrate that the fast clearance is due to disassembly of the ~200 nm nanoparticle into ~30 nm domains that remain soluble and are cleared quickly. We show here that the nanoparticle ultrastructure has a direct impact on in vivo clearance of its cargo i.e. allowing fast release of PFCE, and therefore also bringing the possibility of multifunctional nanoparticle-based imaging to translational imaging, therapy and diagnostics.

Features of magnetorheology of biocompatible chain-forming ferrofluids with multi-core magnetic nanoparticles: Experiment and simulation

We study the magnetorheological properties and structural transitions in novel aqueous colloidal suspensions of magnetic nanoparticles developed for biomedical applications. Defined-shape field-tunable superparamagnetic nanoparticles with clustered cores and their suspensions are produced. The region of intermediate magnetic coupling strength between colloidal ferrofluids and magnetorheological suspensions is systematically studied for the first time. Hybrid numerical simulations with hydrodynamic interactions provide full structural information. The distinctive features of the rheograms are related to transitions between Brownian and persistent microstructure, shape anisotropy, confinement and formation of magnetically coupled gel as a function of relative ratio between thermal, magnetic and hydrodynamic stresses. Non-trivial yielding scenario is observed via the shear banded (delaminated) phase, which may be more widespread in magnetic suspensions than previously thought. Analysis in terms of dimensionless parameters shows generalized behavior, which is applicable to a broad class of magnetic colloids and suspensions.

Magnetic field dependence of the effective magnetic moment of multi-core nanoparticles

The magnetic moment of magnetic nanoparticles (MNPs) is one of the key parameters for various applications. We have experimentally studied the effective magnetic moment of multi-core MNPs and especially their dependence on the applied magnetic field. In contrast to single-core MNPs, the situation is considerably more complex since the effective magnetic moment depends on the size of individual crystallites, their packing density, core configuration, and, thus, the interaction between them. Different approaches to determine the effective magnetic moment are applied for two multi-core MNP systems (FeraSpin XL and BNF Starch). The effective magnetic moment at low magnetic fields is obtained from the ac susceptibility spectra measured at ac field amplitudes up to 9 mT. The obtained values are compared with the high-field values measured at 7 T. In the small-field range (up to 9 mT), a linear field dependence of the effective magnetic moment is found for FeraSpin XL while the value of BNF Starch was found to be nearly constant. The low-field values of both MNP systems are smaller than the values at larger fields, proving the magnetic field dependence of the effective magnetic moment of multi-core MNPs. The estimated values are discussed within a simple model. A consistent picture was found for BNF Starch while the model fails for FeraSpin XL. The different behaviors of both studied multi-core MNP systems are related to the magnetic interactions between the individual crystallites inside a multi-core structure, which are strong for FeraSpin XL due to the high packing density of the crystallites.

Endosomal Confinement of Gold Nanospheres, Nanorods, and Nanoraspberries Governs Their Photothermal Identity and Is Beneficial for Cancer Cell Therapy.

Gold nanoparticles can act as photothermal agents to generate local tumor heating and subsequent depletion upon laser exposure. Herein, photothermal heating of four gold nanoparticles and the resulting induced cancer cell death are systematically assessed, within extra- or intracellular localizations. Two state-of-the-art gold nanorods are compared with small nanospheres (single-core) and nanoraspberries (multicore). Heat generation is measured in water dispersion and in cancer cells, using lasers at wavelengths of 680, 808, and 1064 nm, covering the entire range used in photothermal therapy, defined as near infrared first (NIR-I) and second (NIR-II) windows, with NIR-II offering more tissue penetration. When dispersed in water, gold nanospheres provide no significant heating, gold nanorods are efficient in NIR-I, and only gold nanoraspberries are still heating in NIR-II. However, in cells, due to endosomal confinement, all nanoparticles present an absorption red-shift translating visible and NIR-I absorbing nanoparticles into effective NIR-I and NIR-II nanoheaters, respectively. The gold nanorods then become competitive with the multicore nanoparticles (nanoraspberries) in NIR-II. Similarly, once in cells, gold nanospheres can be envisaged for NIR-I heating. Remarkably, nanoraspberries are efficient nanoheaters, whatever the laser applied, and the extra- versus intra-cellular localization demonstrates treatment versatility.

Relating magnetization, structure and rheology in ferrofluids with multi-core magnetic nanoparticles

Due to their magnetic moments solubilized magnetic nanoparticles are able to spontaneously assemble into dipolar mesostructures, which affect the flow behavior. Multi-core magnetic nanoparticles developed for biomedical applications have enhanced magnetic properties and show significant magnetoviscous effect, but the quantitative interpretation of this phenomenon is incomplete. We apply rheological measurements, magnetic granulometry and dimensional scaling to show the existence of a master curve for magnetorheology of these materials. Using the developed approach the magnetoviscous effect can now be interpreted in a unified way within the stochastic chain model.

Magnetic Nanoparticle Systems for Nanomedicine—A Materials Science Perspective

Iron oxide nanoparticles are the basic components of the most promising magneto-responsive systems for nanomedicine, ranging from drug delivery and imaging to hyperthermia cancer treatment, as well as to rapid point-of-care diagnostic systems with magnetic nanoparticles. Advanced synthesis procedures of single- and multi-core iron-oxide nanoparticles with high magnetic moment and well-defined size and shape, being designed to simultaneously fulfill multiple biomedical functionalities, have been thoroughly evaluated. The review summarizes recent results in manufacturing novel magnetic nanoparticle systems, as well as the use of proper characterization methods that are relevant to the magneto-responsive nature, size range, surface chemistry, structuring behavior, and exploitation conditions of magnetic nanosystems. These refer to particle size, size distribution and aggregation characteristics, zeta potential/surface charge, surface coating, functionalization and catalytic activity, morphology (shape, surface area, surface topology, crystallinity), solubility and stability (e.g., solubility in biological fluids, stability on storage), as well as to DC and AC magnetic properties, particle agglomerates formation, and flow behavior under applied magnetic field (magnetorheology).

Relaxation-based color magnetic particle imaging for viscosity mapping

Magnetic particle imaging (MPI) uses superparamagnetic iron oxide (SPIO) nanoparticles as biomedical imaging tracers. The potential applications of MPI have recently been broadened by the introduction of “color” MPI techniques that can distinguish different nanoparticles and/or environments, e.g., by exploiting the relaxation behavior of SPIOs. One of the important applications of color MPI techniques is viscosity mapping. In this work, we show relaxation-based color MPI experiments that can distinguish the biologically relevant viscosity range of up to 5 mPa s. To find the optimal drive field parameters for viscosity, we compare color MPI results at three different frequencies. We show that frequencies around 10 kHz are well-suited for viscosity mapping using the multicore cluster Nanomag-MIP nanoparticles, providing a one-to-one mapping between the estimated relaxation time constant and viscosity.

Biodegradable magnetic microspheres for drug targeting, temperature controlled drug release, and hyperthermia

Abstract Magnetic microspheres (MMS) used for magnetic drug targeting consist of magnetic nanoparticles (MNP) and a pharmaceutical agent embedded in a polymeric matrix material. The application of MNP for drug targeting enables guiding the MMS to a target area, imaging the position of the MMS with magnetic particle imaging, and finally inducing drug release. As latter takes place by degradation of the MMS or diffusion through the matrix, an increase in temperature, e.g. through magnetic hyperthermia, leads to an accelerated drug release. Here, MMS consisting of poly(lactic-coglycolic) acid (PLGA) with different monomer ratios were prepared by an oil-in-water emulsion evaporation method. The model drug Camptothecin (CPT) and magnetic multicore nanoparticles (MCNP) with a high specific heating rate were embedded into the microspheres. We obtained MMS in the preferred size range of 1 to 2 μm with a concentration of MCNP of 16wt%, a drug load of about 0.5wt% and an excellent heating performance of 161 W/gMMS. Investigations of the drug release behaviour showed an accelerated drug release when increasing the temperature from 20 °C to 37 °C or 43 °C by using a water bath. In addition, an increase in drug release of about 50% through magnetic heating of the MMS up to 44 °C compared to 37 °C was observed. By this, a magnetic hyperthermia induced CPT release from PLGA MMS is demonstrated for the very first time.

Protein corona formation and its constitutional changes on magnetic nanoparticles in serum featuring a polydehydroalanine coating: effects of charge and incubation conditions

The inevitable formation of a protein corona upon contact of nanoparticles with different biological fluids is of great interest in the context of biomedical applications. It is well established that the surface chemistry of the respective nanomaterial has tremendous impact on protein adsorption, both in terms of the actual amount as well as the type of proteins adsorbed. In that regard, especially polyzwitterions are discussed as coating materials as they are known to partially inhibit protein adsorption. We herein present comparative incubation studies on iron oxide nanoparticles (either single core (SPION) or multicore nanoparticles (MCNP)) after coating with either polyanionic or polyzwitterionic polymeric shells based on polydehydroalanine (PDha). Apart from varying surface charge and chemistry, also the influence of incubation time and temperature on the formation and composition of a protein corona upon exposure to fetal calf serum was investigated. The amounts of adsorbed biomolecules were determined using thermogravimetric analysis. SDS-PAGE experiments revealed information on protein composition as major components of the biomolecule corona. Our results show that distinctly lower amounts of proteins are adsorbed onto polyzwitterionic hybrid nanoparticles in general, but also the corona composition varies as indicated by elevated relative ratios of medium molecular weight proteins (i.e. proteins 25–100 kDa) estimated by non-specific silver protein staining. In addition, increasing relative amounts of albumin (67 kDa) via specific Western blot assays on PDha-coated MCNP are detected.